CHEBI:50931 - (Z)-chlorprothixene

Main ChEBI Ontology Automatic Xrefs Reactions Pathways Models
ChEBI Name (Z)-chlorprothixene
ChEBI ID CHEBI:50931
ChEBI ASCII Name (Z)-chlorprothixene
Definition A chlorprothixene in which the double bond adopts a (Z)-configuration.
Stars This entity has been manually annotated by the ChEBI Team.
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Formula C18H18ClNS
Net Charge 0
Average Mass 315.86000
Monoisotopic Mass 315.08485
InChI InChI=1S/C18H18ClNS/c1-20(2)11-5-7-14-15-6-3-4-8-17(15)21-18-10-9-13(19)12-16(14)18/h3-4,6-10,12H,5,11H2,1-2H3/b14-7-
InChIKey WSPOMRSOLSGNFJ-AUWJEWJLSA-N
SMILES [H]\C(CCN(C)C)=C1/c2ccccc2Sc2ccc(Cl)cc12
Roles Classification
Chemical Role(s): Bronsted base
A molecular entity capable of accepting a hydron from a donor (Bronsted acid).
(via organic amino compound )
Biological Role(s): non-narcotic analgesic
A drug that has principally analgesic, antipyretic and anti-inflammatory actions. Non-narcotic analgesics do not bind to opioid receptors.
(via chlorprothixene )
cholinergic antagonist
Any drug that binds to but does not activate cholinergic receptors, thereby blocking the actions of acetylcholine or cholinergic agonists.
(via chlorprothixene )
dopaminergic antagonist
A drug that binds to but does not activate dopamine receptors, thereby blocking the actions of dopamine or exogenous agonists.
(via chlorprothixene )
Application(s): non-narcotic analgesic
A drug that has principally analgesic, antipyretic and anti-inflammatory actions. Non-narcotic analgesics do not bind to opioid receptors.
(via chlorprothixene )
antiemetic
A drug used to prevent nausea or vomiting. An antiemetic may act by a wide range of mechanisms: it might affect the medullary control centres (the vomiting centre and the chemoreceptive trigger zone) or affect the peripheral receptors.
(via chlorprothixene )
sedative
A central nervous system depressant used to induce drowsiness or sleep or to reduce psychological excitement or anxiety.
(via chlorprothixene )
cholinergic antagonist
Any drug that binds to but does not activate cholinergic receptors, thereby blocking the actions of acetylcholine or cholinergic agonists.
(via chlorprothixene )
dopaminergic antagonist
A drug that binds to but does not activate dopamine receptors, thereby blocking the actions of dopamine or exogenous agonists.
(via chlorprothixene )
first generation antipsychotic
Antipsychotic drugs which can have different modes of action but which tend to be more likely than second generation antipsychotics to cause extrapyramidal motor control disabilities such as body rigidity or Parkinson's disease-type movements; such body movements can become permanent even after treatment has ceased.
(via chlorprothixene )
View more via ChEBI Ontology
ChEBI Ontology
Outgoing (Z)-chlorprothixene (CHEBI:50931) is a chlorprothixene (CHEBI:3651)
(Z)-chlorprothixene (CHEBI:50931) is enantiomer of (E)-chlorprothixene (CHEBI:50932)
Incoming (E)-chlorprothixene (CHEBI:50932) is enantiomer of (Z)-chlorprothixene (CHEBI:50931)
IUPAC Name
(3Z)-3-(2-chloro-9H-thioxanthen-9-ylidene)-N,N-dimethylpropan-1-amine
INNs Sources
Chlorprothixenum ChEBI
Clorprotixeno ChEBI
Synonyms Sources
(3Z)-3-(2-chloro-9H-thioxanthen-9-ylidene)-N,N-dimethyl-1-propanamine ChEBI
(Z)-2-Chloro-9-(omega-dimethylaminopropylidene)thioxanthene ChemIDplus
Chlorprothixene ChemIDplus
cis-2-Chloro-9-(3-dimethylaminopropylidene)thioxanthene ChemIDplus
cis-chlorprothixene ChEBI
Manual Xrefs Databases
623 DrugCentral
C07953 KEGG COMPOUND
Chlorprothixene Wikipedia
D00790 KEGG DRUG
DB01239 DrugBank
View more database links
Registry Numbers Types Sources
113-59-7 CAS Registry Number NIST Chemistry WebBook
113-59-7 CAS Registry Number ChemIDplus
9208755 Beilstein Registry Number Beilstein
Citations Waiting for Citations Types Sources
1791531 PubMed citation Europe PMC
24036032 PubMed citation Europe PMC
2444901 PubMed citation Europe PMC
2753075 PubMed citation Europe PMC
2865748 PubMed citation Europe PMC
684078 PubMed citation Europe PMC
Last Modified
23 September 2021